Advertisement
Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
 QUICK SEARCH:   [advanced]


     


Muscle disease

Citations 61-70 of 281 total displayed.

Past content (since Jan 2001):

CLINICAL/SCIENTIFIC NOTES
Homozygous mutation in MYH7 in myosin storage myopathy and cardiomyopathy
Homa Tajsharghi, Anders Oldfors, Dominic P. Macleod, and Michael Swash
Neurology 2007; 68: 962. [Full text] [PDF]  

ARTICLES
Distal arthrogryposis and muscle weakness associated with a ß-tropomyosin mutation
H. Tajsharghi, E. Kimber, D. Holmgren, M. Tulinius, and A. Oldfors
Neurology 2007; 68: 772-775. [Abstract] [Full text] [PDF]  

EDITORIALS
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
Steven A. Greenberg and George W. Padberg
Neurology 2007; 68: 544-545. [Full text] [PDF]  

ARTICLES
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
R. J. Osborne, S. Welle, S. L. Venance, C. A. Thornton, and R. Tawil
Neurology 2007; 68: 569-577. [Abstract] [Full text] [PDF]  

ARTICLES
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4
K. L. Deak, R. J.L.F Lemmers, J. M. Stajich, R. Klooster, R. Tawil, R. R. Frants, M. C. Speer, S. M. van der Maarel, and J. R. Gilbert
Neurology 2007; 68: 578-582. [Abstract] [Full text] [PDF]  

EDITORIALS
Muscle biopsy in patients with myalgia: Still a painful decision
John T. Kissel
Neurology 2007; 68: 170-171. [Full text] [PDF]  

ARTICLES
The role of muscle biopsy in investigating isolated muscle pain
M. Filosto, P. Tonin, G. Vattemi, L. Bertolasi, A. Simonati, N. Rizzuto, and G. Tomelleri
Neurology 2007; 68: 181-186. [Abstract] [Full text] [PDF]  

ARTICLES
Outcome of noninvasive ventilation in children with neuromuscular disease
H. K. Young, A. Lowe, D. A. Fitzgerald, C. Seton, K. A. Waters, E. Kenny, L. S. Hynan, S. T. Iannaccone, K. N. North, and M. M. Ryan
Neurology 2007; 68: 198-201. [Abstract] [Full text] [PDF]  

EDITORIALS
Enzyme replacement for infantile Pompe disease: The first step toward a cure
Kathryn R. Wagner
Neurology 2007; 68: 88-89. [Full text] [PDF]  

ARTICLES
Recombinant human acid {alpha}-glucosidase: Major clinical benefits in infantile-onset Pompe disease
P. S. Kishnani, D. Corzo, M. Nicolino, B. Byrne, H. Mandel, W. L. Hwu, N. Leslie, J. Levine, C. Spencer, M. McDonald, J. Li, J. Dumontier, M. Halberthal, Y. H. Chien, R. Hopkin, S. Vijayaraghavan, D. Gruskin, D. Bartholomew, A. van der Ploeg, J. P. Clancy, R. Parini, G. Morin, M. Beck, G. S. De la Gastine, M. Jokic, B. Thurberg, S. Richards, D. Bali, M. Davison, M. A. Worden, Y. T. Chen, and J. E. Wraith
Neurology 2007; 68: 99-109. [Abstract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page]
Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29

* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
Copyright © 2009 by AAN Enterprises, Inc.
Advertisement